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Direct microcontact printing of oligonucleotides for biochip applications

BACKGROUND: A critical step in the fabrication of biochips is the controlled placement of probes molecules on solid surfaces. This is currently performed by sequential deposition of probes on a target surface with split or solid pins. In this article, we present a cost-effective procedure namely mic...

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Detalles Bibliográficos
Autores principales: Thibault, C, Le Berre, V, Casimirius, S, Trévisiol, E, François, J, Vieu, C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1184096/
https://www.ncbi.nlm.nih.gov/pubmed/15992404
http://dx.doi.org/10.1186/1477-3155-3-7
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author Thibault, C
Le Berre, V
Casimirius, S
Trévisiol, E
François, J
Vieu, C
author_facet Thibault, C
Le Berre, V
Casimirius, S
Trévisiol, E
François, J
Vieu, C
author_sort Thibault, C
collection PubMed
description BACKGROUND: A critical step in the fabrication of biochips is the controlled placement of probes molecules on solid surfaces. This is currently performed by sequential deposition of probes on a target surface with split or solid pins. In this article, we present a cost-effective procedure namely microcontact printing using stamps, for a parallel deposition of probes applicable for manufacturing biochips. RESULTS: Contrary to a previous work, we showed that the stamps tailored with an elastomeric poly(dimethylsiloxane) material did not require any surface modification to be able to adsorb oligonucleotides or PCR products. The adsorbed DNA molecules are subsequently printed efficiently on a target surface with high sub-micron resolution. Secondly, we showed that successive stamping is characterized by an exponential decay of the amount of transferred DNA molecules to the surface up the 4(th )print, then followed by a second regime of transfer that was dependent on the contact time and which resulted in reduced quality of the features. Thus, while consecutive stamping was possible, this procedure turned out to be less reproducible and more time consuming than simply re-inking the stamps between each print. Thirdly, we showed that the hybridization signals on arrays made by microcontact printing were 5 to 10-times higher than those made by conventional spotting methods. Finally, we demonstrated the validity of this microcontact printing method in manufacturing oligonucleotides arrays for mutations recognition in a yeast gene. CONCLUSION: The microcontact printing can be considered as a new potential technology platform to pattern DNA microarrays that may have significant advantages over the conventional spotting technologies as it is easy to implement, it uses low cost material to make the stamp, and the arrays made by this technology are 10-times more sensitive in term of hybridization signals than those manufactured by conventional spotting technology.
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spelling pubmed-11840962005-08-11 Direct microcontact printing of oligonucleotides for biochip applications Thibault, C Le Berre, V Casimirius, S Trévisiol, E François, J Vieu, C J Nanobiotechnology Research BACKGROUND: A critical step in the fabrication of biochips is the controlled placement of probes molecules on solid surfaces. This is currently performed by sequential deposition of probes on a target surface with split or solid pins. In this article, we present a cost-effective procedure namely microcontact printing using stamps, for a parallel deposition of probes applicable for manufacturing biochips. RESULTS: Contrary to a previous work, we showed that the stamps tailored with an elastomeric poly(dimethylsiloxane) material did not require any surface modification to be able to adsorb oligonucleotides or PCR products. The adsorbed DNA molecules are subsequently printed efficiently on a target surface with high sub-micron resolution. Secondly, we showed that successive stamping is characterized by an exponential decay of the amount of transferred DNA molecules to the surface up the 4(th )print, then followed by a second regime of transfer that was dependent on the contact time and which resulted in reduced quality of the features. Thus, while consecutive stamping was possible, this procedure turned out to be less reproducible and more time consuming than simply re-inking the stamps between each print. Thirdly, we showed that the hybridization signals on arrays made by microcontact printing were 5 to 10-times higher than those made by conventional spotting methods. Finally, we demonstrated the validity of this microcontact printing method in manufacturing oligonucleotides arrays for mutations recognition in a yeast gene. CONCLUSION: The microcontact printing can be considered as a new potential technology platform to pattern DNA microarrays that may have significant advantages over the conventional spotting technologies as it is easy to implement, it uses low cost material to make the stamp, and the arrays made by this technology are 10-times more sensitive in term of hybridization signals than those manufactured by conventional spotting technology. BioMed Central 2005-07-01 /pmc/articles/PMC1184096/ /pubmed/15992404 http://dx.doi.org/10.1186/1477-3155-3-7 Text en Copyright © 2005 Thibault et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Thibault, C
Le Berre, V
Casimirius, S
Trévisiol, E
François, J
Vieu, C
Direct microcontact printing of oligonucleotides for biochip applications
title Direct microcontact printing of oligonucleotides for biochip applications
title_full Direct microcontact printing of oligonucleotides for biochip applications
title_fullStr Direct microcontact printing of oligonucleotides for biochip applications
title_full_unstemmed Direct microcontact printing of oligonucleotides for biochip applications
title_short Direct microcontact printing of oligonucleotides for biochip applications
title_sort direct microcontact printing of oligonucleotides for biochip applications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1184096/
https://www.ncbi.nlm.nih.gov/pubmed/15992404
http://dx.doi.org/10.1186/1477-3155-3-7
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